Literature DB >> 106811

The ocular manifestations in Fabry's disease.

N A Sher, R D Letson, R J Desnick.   

Abstract

We present the ocular manifestations in a series of 37 hemizygous male and 25 heterozygous female patients with Fabry's disease. The ocular findings typically do not impair vision, but are unique and diagnostic. Whorl-like corneal deposits were seen in almost all patients and were more severe in the heterozygotes. The lens showed cream-colored anterior capsular deposits, sometimes in striking "propeller" distribution, in one third of the hemizygotes, and in none of the heterozygotes. A faint but unique posterior capsular opacity with a branching radial pattern was seen in 37% of the hemizygotes and 14% of the heterozygotes. Conjunctival vessel aneurysmal dilations and retinal vessel tortuosity were both more frequent and severe in the hemizygotes. Severe visual loss occurred in two hemizygotes as a result of unilateral total central artery occlusions.

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Year:  1979        PMID: 106811     DOI: 10.1001/archopht.1979.01020010327008

Source DB:  PubMed          Journal:  Arch Ophthalmol        ISSN: 0003-9950


  22 in total

1.  Anderson-Fabry disease in Austria.

Authors:  Matthias Lorenz; Anna-Christina Hauser; Margot Püspök-Schwarz; Peter Kotanko; Ingrid Arias; Herbert Zodl; Reinhard Kramar; Eduard Paschke; Till Voigtländer; Gere Sunder-Plassmann
Journal:  Wien Klin Wochenschr       Date:  2003-04-30       Impact factor: 1.704

2.  Ocular manifestations of Fabry's disease: data from the Fabry Outcome Survey.

Authors:  Andrea Sodi; Alexander S Ioannidis; Atul Mehta; Clare Davey; Michael Beck; Suzanne Pitz
Journal:  Br J Ophthalmol       Date:  2006-09-14       Impact factor: 4.638

Review 3.  [HERNS. A rare, hereditary, multisystemic disease with cerebral microangiopathy].

Authors:  C Seifried; M Sitzer; J Jen; G Auburger
Journal:  Nervenarzt       Date:  2005-10       Impact factor: 1.214

4.  Anderson-Fabry disease: clinical manifestations of disease in female heterozygotes.

Authors:  C Whybra; C Kampmann; I Willers; J Davies; B Winchester; J Kriegsmann; K Brühl; A Gal; S Bunge; M Beck
Journal:  J Inherit Metab Dis       Date:  2001-12       Impact factor: 4.982

5.  Mapping the gene for X-linked cataracts and microcornea with facial, dental, and skeletal features to Xp22: an appraisal of the Nance-Horan syndrome.

Authors:  R A Lewis
Journal:  Trans Am Ophthalmol Soc       Date:  1989

6.  Assessment of corneal topographic, tomographic, densitometric, and biomechanical properties of Fabry patients with ocular manifestations.

Authors:  Veysel Cankurtaran; Kemal Tekin; Ayse Idil Cakmak; Merve Inanc; Faruk Hilmi Turgut
Journal:  Graefes Arch Clin Exp Ophthalmol       Date:  2020-01-08       Impact factor: 3.117

Review 7.  Anderson-Fabry disease (angiokeratoma corporis diffusum universale).

Authors:  K W Radcliffe; B A Evans
Journal:  Genitourin Med       Date:  1990-10

8.  Enzyme assay and clinical assessment in subjects with a Chinese hotspot late-onset Fabry mutation (IVS4 + 919G→A).

Authors:  Hsiang-Yu Lin; Cheng-Hung Huang; Hsiao-Chi Yu; Kah-Wai Chong; Ju-Hui Hsu; Pi-Chang Lee; Kang-Hsiang Cheng; Chuan-Chi Chiang; Huey-Jane Ho; Shuan-Pei Lin; Shih-Jen Chen; Po-Kang Lin; Dau-Ming Niu
Journal:  J Inherit Metab Dis       Date:  2010-09-07       Impact factor: 4.982

9.  The microstructure of cornea verticillata in Fabry disease and amiodarone-induced keratopathy: a confocal laser-scanning microscopy study.

Authors:  Karen Falke; Armin Büttner; Michael Schittkowski; Oliver Stachs; Robert Kraak; Andrey Zhivov; Arndt Rolfs; Rudolf Guthoff
Journal:  Graefes Arch Clin Exp Ophthalmol       Date:  2008-10-18       Impact factor: 3.117

10.  Fabry disease in children and the effects of enzyme replacement treatment.

Authors:  Guillem Pintos-Morell; Michael Beck
Journal:  Eur J Pediatr       Date:  2009-02-26       Impact factor: 3.183

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